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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DC43114 | cis-Miyabenol C |
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| DC43113 | Rubelloside B |
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| DC43112 | 3-Epidehydrotumulosic acid |
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| DC43111 | (-)-SW203668 Hydrochloride |
More potent enantiomer of SW203668 (AOB9773), a novel tumor-specific inhibitor of stearoyl CoA desaturase (SCD)
More description
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| DC43110 | 9-O-Feruloyl-5,5'-dimethoxylariciresinol |
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| DC43107 | Brevilin A |
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| DC43106 | Calyxin B |
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| DC43105 | I-XW-053 sodium salt |
Novel capsid targeted inhibitor of HIV-1 replication
More description
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| DC43104 | Clerodenoside A |
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| DC43103 | Kaempferol-3-O-(6''-O-cis-coumaryl)glucoside |
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| DC43102 | Piroheptine Hydrochloride |
Antiparkinsonian
More description
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| DC43100 | ML345 |
Inhibitor of the Insulin-Degrading Enzyme (IDE)
More description
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| DC43099 | SR-2959 |
Inhibitor of the Insulin-Degrading Enzyme (IDE)
More description
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| DC43098 | Yunnancoronarin A |
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| DC43097 | Kaempferol tetraacetate |
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| DC43096 | Myriceric acid C |
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| DC43095 | 2,3,8-Tri-O-methylellagic acid |
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| DC43094 | Simiarenol |
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| DC43093 | PF-05274857 HCl |
Very potent inhibitor, with an IC50 of less than 10 nM for VEGFR2, MET, Kit and FLT3-ITD
More description
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| DC43092 | ML318 |
Novel inhibitor of Pseudomonas aeruginosa PvdQ acylase, an enzyme involved in siderophore pyoverdine synthesis
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| DC43091 | Villosin C |
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| DC43090 | Villosin |
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| DC43089 | 3',5,5',7-Tetrahydroxyflavanone |
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| DC43087 | Sambutoxin |
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| DC43086 | BMS-466442 |
The first selective inhibitor of the amino acid transporter alanine serine cysteine transporter-1 (asc-1)
More description
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| DC43085 | Cariporide Mesylate |
Selective Na+/H+ exchanger isoform 1 (NHE1) inhibitor
More description
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| DC43084 | 3-O-(2'E ,4'Z-decadienoyl)-20-O-acetylingenol |
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| DC43083 | CMF-019 |
The first potent biased small molecule agonist at the apelin receptor, increasing cardiac contractility in vivo
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| DC43082 | Catalpalactone |
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| DC43081 | Inz-5 |
Novel Stable Fungal-Selective Inhibitor of Mitochondrial Cytochrome bc1
More description
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